Recall Z-2129-2017— Teleflex Medical
Class II · Terminated
Class II FDA medical device recall by Teleflex Medical, initiated 2017-04-21, terminated 2020-01-27. FDA's recall record names no specific 510(k) clearance for this event. Product: PE CONNECTOR 5 IN 1 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory. Reason: Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used..
- Recalling firm
- Teleflex Medical
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-04-21
- Terminated
- 2020-01-27
- Firm location
- Research Triangle Park, NC, United States
Product description
PE CONNECTOR 5 IN 1 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory
Reason for recall
Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.
Data sourced from openFDA. This site is unofficial and independent of the FDA.